首页> 外文期刊>Behavioural Brain Research: An International Journal >Antipsychotic drugs reverse MK-801-induced cognitive and social interaction deficits in zebrafish (Danio rerio).
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Antipsychotic drugs reverse MK-801-induced cognitive and social interaction deficits in zebrafish (Danio rerio).

机译:抗精神病药可以逆转MK-801引起的斑马鱼(Danio rerio)认知和社交互动缺陷。

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摘要

Schizophrenia is a severe mental illness characterized by positive and negative symptoms and cognitive deficits. Reduction of glutamatergic neurotransmission by NMDA receptor antagonists mimics symptoms of schizophrenia. Modeling social interaction and cognitive impairment in animals can be of great benefit in the effort to develop novel treatments for negative and cognitive symptoms of schizophrenia. Studies have demonstrated that these behavioral changes are, in some cases, sensitive to remediation by antipsychotic drugs. The zebrafish has been proposed as a candidate to study the in vivo effects of several drugs and to discover new pharmacological targets. In the current study we investigated the ability of antipsychotic drugs to reverse schizophrenia-like symptoms produced by the NMDA receptor antagonist MK-801. Results showed that MK-801 (5muM) given pre-training hindered memory formation while both atypical antipsychotics sulpiride (250muM) and olanzapine (50muM) improved MK-801-induced amnesia. The same change was observed in the social interaction task, where atypical antipsychotics reversed the MK-801-induced social interaction deficit whereas the typical antipsychotic haloperidol (9muM) was ineffective to reverse those behavioral deficits. Therefore, MK-801-treated zebrafish showed some behavioral features observed in schizophrenia, such as cognitive and social interaction deficits, which were reverted by current available atypical drugs.
机译:精神分裂症是一种严重的精神疾病,其特征是阳性和阴性症状和认知缺陷。 NMDA受体拮抗剂降低谷氨酸能神经传递可模拟精神分裂症的症状。在动物中建立社交互动和认知障碍模型可以为开发针对精神分裂症的阴性和认知症状的新疗法提供巨大帮助。研究表明,在某些情况下,这些行为改变对抗精神病药物的治疗敏感。斑马鱼已被提议作为候选药物来研究几种药物的体内作用并发现新的药理学靶标。在本研究中,我们研究了抗精神病药逆转NMDA受体拮抗剂MK-801所产生的精神分裂症样症状的能力。结果显示,预先训练的MK-801(5μM)阻碍了记忆形成,而非典型抗精神病药舒必利(250μM)和奥氮平(50μM)均可改善MK-801引起的健忘症。在社交互动任务中观察到了相同的变化,其中非典型的抗精神病药逆转了MK-801引起的社交互动缺陷,而典型的抗精神病药物氟哌啶醇(9μM)不能有效地逆转这些行为缺陷。因此,用MK-801处理的斑马鱼表现出在精神分裂症中观察到的某些行为特征,例如认知和社交互动缺陷,这些缺陷已被当前可用的非典型药物所弥补。

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